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Hair Cell Bundles: Flexoelectric Motors of the Inner Ear

Microvilli (stereocilia) projecting from the apex of hair cells in the inner ear are actively motile structures that feed energy into the vibration of the inner ear and enhance sensitivity to sound. The biophysical mechanism underlying the hair bundle motor is unknown. In this study, we examined a m...

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Detalles Bibliográficos
Autores principales: Breneman, Kathryn D., Brownell, William E., Rabbitt, Richard D.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668172/
https://www.ncbi.nlm.nih.gov/pubmed/19384413
http://dx.doi.org/10.1371/journal.pone.0005201
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author Breneman, Kathryn D.
Brownell, William E.
Rabbitt, Richard D.
author_facet Breneman, Kathryn D.
Brownell, William E.
Rabbitt, Richard D.
author_sort Breneman, Kathryn D.
collection PubMed
description Microvilli (stereocilia) projecting from the apex of hair cells in the inner ear are actively motile structures that feed energy into the vibration of the inner ear and enhance sensitivity to sound. The biophysical mechanism underlying the hair bundle motor is unknown. In this study, we examined a membrane flexoelectric origin for active movements in stereocilia and conclude that it is likely to be an important contributor to mechanical power output by hair bundles. We formulated a realistic biophysical model of stereocilia incorporating stereocilia dimensions, the known flexoelectric coefficient of lipid membranes, mechanical compliance, and fluid drag. Electrical power enters the stereocilia through displacement sensitive ion channels and, due to the small diameter of stereocilia, is converted to useful mechanical power output by flexoelectricity. This motor augments molecular motors associated with the mechanosensitive apparatus itself that have been described previously. The model reveals stereocilia to be highly efficient and fast flexoelectric motors that capture the energy in the extracellular electro-chemical potential of the inner ear to generate mechanical power output. The power analysis provides an explanation for the correlation between stereocilia height and the tonotopic organization of hearing organs. Further, results suggest that flexoelectricity may be essential to the exquisite sensitivity and frequency selectivity of non-mammalian hearing organs at high auditory frequencies, and may contribute to the “cochlear amplifier” in mammals.
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spelling pubmed-26681722009-04-22 Hair Cell Bundles: Flexoelectric Motors of the Inner Ear Breneman, Kathryn D. Brownell, William E. Rabbitt, Richard D. PLoS One Research Article Microvilli (stereocilia) projecting from the apex of hair cells in the inner ear are actively motile structures that feed energy into the vibration of the inner ear and enhance sensitivity to sound. The biophysical mechanism underlying the hair bundle motor is unknown. In this study, we examined a membrane flexoelectric origin for active movements in stereocilia and conclude that it is likely to be an important contributor to mechanical power output by hair bundles. We formulated a realistic biophysical model of stereocilia incorporating stereocilia dimensions, the known flexoelectric coefficient of lipid membranes, mechanical compliance, and fluid drag. Electrical power enters the stereocilia through displacement sensitive ion channels and, due to the small diameter of stereocilia, is converted to useful mechanical power output by flexoelectricity. This motor augments molecular motors associated with the mechanosensitive apparatus itself that have been described previously. The model reveals stereocilia to be highly efficient and fast flexoelectric motors that capture the energy in the extracellular electro-chemical potential of the inner ear to generate mechanical power output. The power analysis provides an explanation for the correlation between stereocilia height and the tonotopic organization of hearing organs. Further, results suggest that flexoelectricity may be essential to the exquisite sensitivity and frequency selectivity of non-mammalian hearing organs at high auditory frequencies, and may contribute to the “cochlear amplifier” in mammals. Public Library of Science 2009-04-22 /pmc/articles/PMC2668172/ /pubmed/19384413 http://dx.doi.org/10.1371/journal.pone.0005201 Text en Breneman et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Breneman, Kathryn D.
Brownell, William E.
Rabbitt, Richard D.
Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title_full Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title_fullStr Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title_full_unstemmed Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title_short Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
title_sort hair cell bundles: flexoelectric motors of the inner ear
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668172/
https://www.ncbi.nlm.nih.gov/pubmed/19384413
http://dx.doi.org/10.1371/journal.pone.0005201
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